Associate Scientist I - Quality Control, MQC

Associate Scientist I – Quality Control, MQC

Position Summary:

• Work Schedule: 4x10 Wednesday – Saturday AM
• 100% on-site
• Madison, WI

Catalent Madison is a pharmaceutical manufacturing site specializing in the development and production of high-quality drug products, with a strong focus on biologics and sterile injectables. The site supports global clients by delivering compliant, reliable, and scalable manufacturing solutions.

The Associate Scientist - Quality Control at Catalent Madison is responsible for performing and documenting cGMP testing on products, raw materials, and the manufacturing environment to ensure quality and compliance standards are met. The Associate Scientist I – Quality Control involves operating lab equipment, supporting environmental monitoring, maintaining laboratory systems (LIMS), and contributing to routine lab maintenance and continuous GMP compliance.

The Role:

• Performs cGMP Quality Control testing and documents results under supervision
• Operates basic QC laboratory equipment and performs routine maintenance
• Reviews analytical data for accuracy, completeness, and SOP compliance
• Enters and manages data in LIMS and laboratory reporting systems
• Prepares solutions and stages materials for QC lab activities
• Conducts environmental monitoring (air, surface, personnel, gas, and water sampling)
• Logs and tracks samples using laboratory systems
• Maintains lab organization and cleanliness in alignment with 5S standards
• Other duties as assigned

The Candidate:

•  Bachelor’s Degree in Biology, Biotechnology, Chemistry or related life sciences field; OR Associate Degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 1 year of industry experience; OR High School Diploma or equivalent with a minimum of 4 years of industry experience.
• Basic understanding of analytical chemistry and simple lab equipment preferred
• Familiarity with clean room procedure, aseptic technique, and general lab equipment experience.
• cGMP, Good Documentation Practices (GDP) or Good Laboratory Practices (GLP) knowledge preferred
• Following standard operating procedures (SOP) preferred
• General laboratory equipment experience, including micropipettes preferred

Why you should join Catalent:

• Potential for career growth on an expanding team
• Abundance of cross-functional exposure to other areas within the organization
• 152 hours of paid time off annually + 8 paid holidays
• Day one benefits! Medical, dental, vision and 401K benefits effective on your first day

Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsol